Amikacin spectrum of activity is the broadest of all aminoglycosides.Amikacin is active against most strains of Serratia, Proteus, and Pseudomonas aeruginosa as well as most strains of Klebsiella, Enterobacter, and Escherichia coli that are resistant to gentamicin and tobramycin and is rapidly bactericidal.Amikacin doses are 15 mg/kg once-daily, and 7.5 mg/kg twice-daily in infants, and 20 to 40 mg/kg once-daily in children.Amikacin is preferentially administered once-daily, because yields lower though and higher peak concentrations, thus reducing the risks of toxicity, and increases peak concentration, thus improving therapeutic efficacy.Amikacin is absorbed rapidly after intramuscular injection; its peak plasma concentration is 20 µg/ml after an injection of 7.5 mg/kg.Amikacin mean half-lives are 6.0 hours in infants in the first weeks of life, and 1.9 hours in children aged up to 6 years.Amikacin causes limited ototoxicity and nephrotoxicity in infants and children.After a single intramuscular amikacin dose of 7.5 mg/kg, its concentration (µg/ml) is 14.9 in serum, 2.2 in skeletal muscle, and 1.9 in fat tissue.Because of its polar nature, amikacin penetrates poorly into the cerebrospinal fluid, and serum peak to amniotic fluid ratio is 0.03.Amikacin pharmacokinetics have been extensively studied in infants and children and pharmacokinetic parameters vary remarkably.Half-life and clearance decreases and increases, respectively, during infant maturation.Burn, cancer and renal impairment have an important impact on pharmacokinetics.Some bacteria may become resistant to amikacin.The aim of this study is to review the published data on amikacin effects, metabolism, pharmacokinetics, and bacteria-resistance in infants and children.